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GWAS Study

Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women.

Adedokun B, Du Z, Gao G et al.

34234117 PubMed ID
GWAS Study Type
248385 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AB
Adedokun B
DZ
Du Z
GG
Gao G
AT
Ahearn TU
LK
Lunetta KL
ZG
Zirpoli G
FJ
Figueroa J
JE
John EM
BL
Bernstein L
ZW
Zheng W
HJ
Hu JJ
ZR
Ziegler RG
NS
Nyante S
BE
Bandera EV
IS
Ingles SA
PM
Press MF
DS
Deming-Halverson SL
RJ
Rodriguez-Gil JL
YS
Yao S
OT
Ogundiran TO
OO
Ojengbede O
BW
Blot W
TM
Troester MA
NK
Nathanson KL
HA
Hennis A
NB
Nemesure B
AS
Ambs S
FP
Fiorica PN
SL
Sucheston-Campbell LE
BJ
Bensen JT
KL
Kushi LH
TG
Torres-Mejia G
HD
Hu D
FL
Fejerman L
BM
Bolla MK
DJ
Dennis J
DA
Dunning AM
ED
Easton DF
MK
Michailidou K
PP
Pharoah PDP
WQ
Wang Q
SD
Sandler DP
TJ
Taylor JA
OK
O'Brien KM
KC
Kitahara CM
FA
Falusi AG
BC
Babalola C
YJ
Yarney J
AB
Awuah B
AB
Addai-Wiafe B
CS
Chanock SJ
OA
Olshan AF
AC
Ambrosone CB
CD
Conti DV
ZE
Ziv E
OO
Olopade OI
GM
Garcia-Closas M
PJ
Palmer JR
HC
Haiman CA
HD
Huo D
Chapter II

Abstract

Summary of the research findings

Our study describes breast cancer risk loci using a cross-ancestry GWAS approach. We first identify variants that are associated with breast cancer at P < 0.05 from African ancestry GWAS meta-analysis (9241 cases and 10193 controls), then meta-analyze with European ancestry GWAS data (122977 cases and 105974 controls) from the Breast Cancer Association Consortium. The approach identifies four loci for overall breast cancer risk [1p13.3, 5q31.1, 15q24 (two independent signals), and 15q26.3] and two loci for estrogen receptor-negative disease (1q41 and 7q11.23) at genome-wide significance. Four of the index single nucleotide polymorphisms (SNPs) lie within introns of genes (KCNK2, C5orf56, SCAMP2, and SIN3A) and the other index SNPs are located close to GSTM4, AMPD2, CASTOR2, and RP11-168G16.2. Here we present risk loci with consistent direction of associations in African and European descendants. The study suggests that replication across multiple ancestry populations can help improve the understanding of breast cancer genetics and identify causal variants.

9,241 African ancestry cases, 10,193 African ancestry controls, 122,977 European ancestry cases, 105,974 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

248385
Total Participants
GWAS
Study Type
No
Replicated
African unspecified, European
Ancestry
Chapter IV

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